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Treatment of neuropathic pain with n-methyl-d-aspartate (NMDA) receptor antagonists

a technology of nephropathy and receptor antagonists, which is applied in the direction of drug compositions, peptide/protein ingredients, and metabolic disorders, can solve the problems of reducing the attractiveness of analgesics to the human body, ineffective relief ineffective treatment of chronic central neuropathic pain, etc., to achieve effective treatment and reduce the severity of central neuropathic pain, no

Inactive Publication Date: 2013-05-16
ANALGESIC NEUROPHARMLS
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The invention is a method of treating chronic neuropathic pain in individuals with spinal cord injuries using NMDA receptor antagonists. The method offers efficient pain relief with reduced side effects such as fatigue, confusion, and speech difficulty. It can also reduce the severity of central neuropathic pain in spinal cord injury patients who have pain in the central nervous system. This treatment offers an effective way to manage pain in humans with spinal cord injuries.

Problems solved by technology

However, standard analgesics, such as nonsteroidal anti-inflammatory drugs, opioids, tricyclic antidepressants, anticonvulsants and antispasmodics, are ineffective in relieving the chronic central neuropathic pain, in particular pain associated with spinal cord injury.
Further, relief of pain by certain analgesics can result in adverse side effects such as fatigue, confusion, dizziness, somnolence and speech difficulty thereby diminishing the attractiveness of the analgesic to the human.

Method used

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  • Treatment of neuropathic pain with n-methyl-d-aspartate (NMDA) receptor antagonists
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  • Treatment of neuropathic pain with n-methyl-d-aspartate (NMDA) receptor antagonists

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Embodiment Construction

[0018]The features and other details of the invention, either as steps of the invention or as combinations of parts of the invention, will now be more particularly described and pointed out in the claims. It will be understood that the particular embodiments of the invention are shown by way of illustration and not as limitations of the invention. The principle features of this invention can be employed in various embodiments without departing from the scope of the invention.

[0019]The present invention relates to the discovery that treatment with NMDA receptor antagonists decrease central neuropathic pain of humans. In particular, the chronic administration of an NMDA receptor antagonist (e.g., dextromethorphan hydrobromide) has been found to decrease chronic central neuropathic pain in humans following spinal cord injury with no or significantly diminished side effects.

[0020]The NMDA receptor antagonists can be high affinity NMDA receptor antagonists (e.g., ketamine), low affinity ...

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Abstract

Central neuropathic pain is treated with an analgesic composition that consists essentially of an N-methyl-D-aspartate (NMDA) receptor antagonist. In one embodiment, the invention includes chronic administration of the (NMDA) receptor antagonist. In another embodiment, the invention is use of an NMDA receptor antagonist or component thereof for the manufacture of a medicament than includes an analgesic component that consists essentially of an NMDA receptor antagonist for the chronic treatment of central neuropathic pain.

Description

RELATED APPLICATION[0001]This application claims the benefit of U.S. Provisional Application “Treatment of Neuropathic Pain with N-Methyl-D-Aspartate (NMDA) Receptor Antagonists” by Christine N. Sang (Attorney Docket Number 0838.2002-000), filed Jun. 7, 2001, the entire teachings of which are incorporated herein by reference.BACKGROUND OF THE INVENTION[0002]Humans with injury to the central nervous system (e.g., brain and spinal cord) can suffer from chronic central neuropathic pain. However, standard analgesics, such as nonsteroidal anti-inflammatory drugs, opioids, tricyclic antidepressants, anticonvulsants and antispasmodics, are ineffective in relieving the chronic central neuropathic pain, in particular pain associated with spinal cord injury. Further, relief of pain by certain analgesics can result in adverse side effects such as fatigue, confusion, dizziness, somnolence and speech difficulty thereby diminishing the attractiveness of the analgesic to the human. Thus, there is ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/485A61K31/195A61K31/00A61K31/197A61K31/198A61K45/08A61P25/04
CPCA61K31/00A61K31/197A61K31/198A61K31/485A61K31/496A61K31/195A61K45/06A61K2300/00A61P25/04A61P3/04A61P3/06A61P43/00A61P3/10
Inventor SANG, CHRISTINE N.
Owner ANALGESIC NEUROPHARMLS
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